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Variant (rsID / SNP)

rs7406119

B3GNTL1

rs7406119 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to B3GNTL1. Location: chromosome 17, position 81,006,629. The table records no clinical significance for this variant.

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Reference-table entries

B3GNTL1Not classified
Variant type
synonymous_variant
Chromosome / position
17:81006629
HGVS
NM_001320742.2,c.51G>A,p.Pro17Pro
Allele change
Synonymous_P17P

Public references

Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.